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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589955Generated: October 30, 2026

Water → Tert-butyl 4-[8-(cyclobutylsulfamoyl)-5,8-diazaspiro[2.5]octan-5-yl]pyrrolo[2,3-d]pyrimidine-7-carboxylate

https://huagongshe.com/reaction/589955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantN-cyclobutyl-5-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-5,8-diazaspiro[2.5]octane-8-sulfonamideHCID 68296040—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-[8-(cyclobutylsulfamoyl)-5,8-diazaspiro[2.5]octan-5-yl]pyrrolo[2,3-d]pyrimidine-7-carboxylateHCID 68295998—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-cyclobutyl-5-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-5,8-diazaspiro[2.5]octane-8-sulfonamide (intermediate 30) (4.4 mmol) was dissolved in dry DMF (15 ml), added K2CO3 (5.28 mmol) and cooled to 0° C. A solution of BOC2O (1.06 g, 4.86 mmol) in dry DMF (5 mL) was added and the reaction mixture was allowed to warm up freely to rt and stirred at rt for 16 h. The crude mixture was treated with water (150 mL) and extracted with EtOAc (3×100 mL). The combined organic phases were washed with H2O (2×50 mL), brine (2×50 mL), dried over Na2SO4, filtered and concentrated in vacuo. The product was purified by flash chromatography on silica using EtOAc in heptane as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233964B2
Source datasetuspto-grants-2016_01
ORD IDord-18381497fddd43069792b489804e8341
Source noteuspto-grants-2016_01